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Assessing the capability of massively parallel sequencing for opportunistic pharmacogenetic screening

PURPOSE: To assess exome data for pre-emptive pharmacogenetic screening for 203 clinically-relevant pharmacogenetic variant positions from the Pharmacogenomics Knowledgebase and Clinical Pharmacogenetics Implementation Consortium and identify copy number variants (CNVs) in CYP2D6. METHODS: We examin...

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Detalles Bibliográficos
Autores principales:	Ng, David, Hong, Celine S., Singh, Larry N., Johnston, Jennifer J., Mullikin, James C., Biesecker, Leslie G.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	2016
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5316383/ https://www.ncbi.nlm.nih.gov/pubmed/27537706 http://dx.doi.org/10.1038/gim.2016.105

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